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News
LLS TAP announces five new investments supporting next generation immunotherapies
RYE BROOK, N.Y., April 22, 2021 /PRNewswire/ -- The Leukemia & Lymphoma Society Therapy Acceleration Program® (LLS TAP) today announced five new inves…
News
LLS Statement on Anti-Asian Violence and Discrimination
The Leukemia & Lymphoma Society condemns violence and discrimination against members of the Asian, Asian American, and Pacific Islander community, whi…
News
FDA Approves Isatuximab for Relapsed/Refractory Multiple Myeloma
The U.S. Food and Drug Administration (FDA) approved isatuximab (Sarclisa) in combination with carfilzomib and dexamethasone to treat adult patients w…
News
Everyday Heroes Fight for a Cancer-Free Future
The Leukemia & Lymphoma Society kicks-off 32nd annual Man & Woman of the Year campaign bringing together diverse communities across the country
Research
Publication of CPX-351 Clinical Data in 'Blood Advances': Phase 3 Post-Hoc Analyses
March 16, 2021 - CPX-351 (Vyxeos, daunorubicin and cytarabine liposome for injection) is a dual-drug liposomal encapsulation of daunorubicin and cytar…
Research
FDA Approves Vyxeos for Secondary Acute Myeloid Leukemia in Children
DUBLIN, March 30, 2021 - Jazz Pharmaceuticals plc (Nasdaq: JAZZ) announced that the U.S. Food and Drug Administration (FDA) approved a revised label f…
Research
Age-Related AML Risk: An Exploration of Hematopoietic Stem Cell Epigenetics
The population of elderly people is increasing both in the United States and worldwide, and this increase presents challenges in addressing the medica…
Research
Genotyping of Transcriptomes: A Breakthrough Technology in Single-Cell Analysis
Though a patient’s cancer is treated as a single disease, it is made up of a diverse collection of cells that are related but may have distinct charac…
Research
Sports Analytics Model Adapted to Improve Cancer Outcome Prediction
Outcome prediction is central to the care of cancer patients. Will the patient be symptom-free at some point in the near future or succumb to the dise…
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